
Phlexglobal, a PharmaLex company now part of Cencora, is a global authority in Trial Master File (TMF) services and technology. It offers next-generation AI-powered eTMF software, PhlexTMF, which reduces document misfiles and metadata errors to improve TMF quality and inspection readiness. The company combines expert services with innovative technology to help pharmaceutical sponsors and CROs achieve high standards of TMF completeness, timeliness, and quality. Phlexglobal supports clinical trial management with a comprehensive suite of software and expert services, including TMF quality review, heatmaps, migrations, and study owner support. It has a strong market position with hundreds of clients worldwide and a team of over 150 experts, helping companies reduce inspection risk and improve regulatory compliance.

Phlexglobal, a PharmaLex company now part of Cencora, is a global authority in Trial Master File (TMF) services and technology. It offers next-generation AI-powered eTMF software, PhlexTMF, which reduces document misfiles and metadata errors to improve TMF quality and inspection readiness. The company combines expert services with innovative technology to help pharmaceutical sponsors and CROs achieve high standards of TMF completeness, timeliness, and quality. Phlexglobal supports clinical trial management with a comprehensive suite of software and expert services, including TMF quality review, heatmaps, migrations, and study owner support. It has a strong market position with hundreds of clients worldwide and a team of over 150 experts, helping companies reduce inspection risk and improve regulatory compliance.
Founded: 2013 (Munich, Germany)
Specialization: Regulatory Information Management (RIM), IDMP, eCTD, ML-based document/data extraction
Acquisition: Acquired by Phlexglobal in January 2020
Team size (reported): Over 150 experts referenced within combined Phlexglobal context
Regulatory document management and automation for life sciences (improving data extraction, regulatory submission formatting, and compliance).
2013
Life sciences / Regulatory information management
Total Funding: 0.00 USD